A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3634832



Internal ID7021632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:69065839..69069009hg38UCSC Ensembl
Innerchr14:69065839..69069009hg38UCSC Ensembl
Outerchr14:69065635..69069136hg38UCSC Ensembl
chr14:69532556..69535726hg19UCSC Ensembl
Innerchr14:69532556..69535726hg19UCSC Ensembl
Outerchr14:69532352..69535853hg19UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg383171
hg193171
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15051762
SamplesNA18620
Known GenesDCAF5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3634832
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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